drugset / Trial / NCT01437059

Trial to Evaluate Safety and Tolerability of ALN-PCS02 in Subjects With Elevated LDL-Cholesterol (LDL-C)

NCT01437059 ↗

Phase 1 Completed 32 enrolled Alnylam Pharmaceuticals
RandomizedParallel-groupSingle-blindTreatment

Summary

The purpose of this study is to determine the safety, tolerability, pharmacokinetics and pharmacodynamics of a single dose of ALN-PCS02 in subjects with Elevated LDL-Cholesterol (LDL-C).

Timeline

Start
2011-09
Primary completion
2012-03
Completion
2012-09

Drugs

EvaluationDrugModalityDoseRoute
Comparator ALN-PCS02 Unknown 0.015 mg/kg Intravenous
Comparator ALN-PCS02 Unknown 0.045 mg/kg Intravenous
Comparator ALN-PCS02 Unknown 0.09 mg/kg Intravenous
Comparator ALN-PCS02 Unknown 0.15 mg/kg Intravenous
Comparator ALN-PCS02 Unknown 0.25 mg/kg Intravenous
Comparator ALN-PCS02 Unknown 0.4 mg/kg Intravenous